Canonical Allele Identifier: CA382892604

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895578G>C (hg19) ; chr11:g.119024868G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024868G>C , CM000673.2:g.119024868G>C	GRCh38
NC_000011.9:g.118895578G>C , CM000673.1:g.118895578G>C	GRCh37
NC_000011.8:g.118400788G>C	NCBI36
NG_013331.1:g.11038C>G , LRG_187:g.11038C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1542C>G (SLC37A4)
ENST00000697845.1:n.2531C>G (SLC37A4)
ENST00000697846.1:n.1904C>G (SLC37A4)
ENST00000697847.1:n.1615C>G (SLC37A4)
ENST00000697849.1:n.4008C>G (SLC37A4)
ENST00000697850.1:n.2199C>G (SLC37A4)
ENST00000697851.1:n.3170C>G (SLC37A4)
ENST00000638186.1:n.1636C>G (SLC37A4)
ENST00000638360.1:n.1468C>G (SLC37A4)
ENST00000638925.1:n.1601C>G (SLC37A4)
ENST00000650539.1:n.1804C>G (SLC37A4)
ENST00000330775.9:c.*42C>G (SLC37A4)	ENSP00000476242.2:n.*42C>G
ENST00000357590.9:c.*42C>G (SLC37A4)	ENSP00000476176.2:n.*42C>G
ENST00000525102.5:n.2090C>G (SLC37A4)
ENST00000526275.5:n.2114C>G (SLC37A4)
ENST00000527992.5:n.1560C>G (SLC37A4)
ENST00000532085.1:n.5350C>G (SLC37A4)
ENST00000533058.5:c.593G>C (TRAPPC4)	ENSP00000432920.1:p.Gly198Ala
ENST00000538950.5:c.*42C>G (SLC37A4)	ENSP00000475991.2:n.*42C>G
ENST00000545985.5:c.*42C>G (SLC37A4)	ENSP00000475241.2:n.*42C>G
NM_001164277.1:c.*42C>G , LRG_187t1:c.*42C>G (SLC37A4)	NP_001157749.1:n.*42C>G
NM_001164278.1:c.*42C>G (SLC37A4)	NP_001157750.1:n.*42C>G
NM_001164279.1:c.*42C>G (SLC37A4)	NP_001157751.1:n.*42C>G
NM_001164280.1:c.*42C>G (SLC37A4)	NP_001157752.1:n.*42C>G
NM_001467.5:c.*42C>G (SLC37A4)	NP_001458.1:n.*42C>G
NM_001164278.2:c.*42C>G (SLC37A4)	NP_001157750.1:n.*42C>G
NM_001164279.2:c.*42C>G (SLC37A4)	NP_001157751.1:n.*42C>G
NM_001164280.2:c.*42C>G (SLC37A4)	NP_001157752.1:n.*42C>G
NM_001467.6:c.*42C>G (SLC37A4)	NP_001458.1:n.*42C>G
NM_001164277.2:c.*42C>G (SLC37A4) MANE Select	NP_001157749.1:n.*42C>G